A new and mild method for the reduction of secondary amides to carbinolamine ethers and imines: a conversion of oxotomaymycin to tomaymycin
- 1 January 1983
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 24 (47) , 5165-5168
- https://doi.org/10.1016/s0040-4039(00)88387-2
Abstract
No abstract availableKeywords
This publication has 14 references indexed in Scilit:
- Prothracarcin, a novel antitumor antibiotic.The Journal of Antibiotics, 1982
- Synthesis of 7,9-di-O-methyl-11-oxosibiromycinoneThe Journal of Organic Chemistry, 1981
- Mazethramycin, a new member of anthramycin group antibiotics.The Journal of Antibiotics, 1980
- Mild and Efficient Methods for the Reductive Cleavage of Nitrogen-Oxygen BondsSynthetic Communications, 1979
- Conversion of imidoyl chlorides to imines. A new method for the acyl exchange and cleavage of amidesTetrahedron Letters, 1978
- Pyrrolo(1,4)benzodiazepine antitumor antibiotics. Comparative aspects of anthramycin, tomaymycin and sibiromycin.The Journal of Antibiotics, 1977
- 2-Thiazolines in organic synthesis. Synthesis of mono-, di-, and trialkylacetaldehydesThe Journal of Organic Chemistry, 1975
- Total synthesis of anthramycinJournal of the American Chemical Society, 1968
- The Structure of AnthramycinJournal of the American Chemical Society, 1965
- α, β‐ungesättigte Aldehyde, III. Mitteil.: Die zwei Cyclocitryliden‐acetaldehydeBerichte der deutschen chemischen Gesellschaft (A and B Series), 1937